HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926851Generated: October 28, 2026
tert-Butyl acrylate → 3-((3-Tert-butoxy-3-oxopropylthio)methyl)benzoic acid
https://huagongshe.com/reaction/926851
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-(mercaptomethyl)benzoic acid | HCID 11321189 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-((3-Tert-butoxy-3-oxopropylthio)methyl)benzoic acid | HCID 66586713 | 47% |
Reaction Steps
Into a 500-mL round bottom flask, was placed a solution of 3-(mercaptomethyl)benzoic acid (12 g, 71.43 mmol, 1.00 equiv) in acetonitrile (200 mL), tert-butyl acrylate (60 mL), and DBU (21.7 g, 142.76 mmol, 2.00 equiv). The resulting solution was stirred overnight at 80° C. in an oil bath. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 200 mL of water and adjusted to pH 2-3 with 10% hydrochloric acid. The resulting solution was extracted with 3×200 mL of ethyl acetate and the organic layers combined. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with petroleum ether/ethyl acetate (50:1) to give 10.5 g (47%) of 3-((3-tert-butoxy-3-oxopropylthio)methyl)benzoic acid as red oil. 1H-NMR (300 MHz, CDCl3, ppm): δ 8.08 (s, 1H), 8.04 (d, J=7.8 Hz, 1H), 7.62 (d, J=7.8 Hz, 1H), 7.46 (t, 1H), 3.81 (s, 2H), 2.68 (t, 2H), 2.50 (t, 2H), 1.48 (s, 9H). MS (ES, m/z): 295 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09289430B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-e46b39b16db141d6999e1001edf6328a |
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| Source note | uspto-grants-2016_03 |
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